Results 61 to 70 of about 1,825 (178)

Automatic Detection of Exudate in Diabetic Retinopathy Using K-Clustering Algorithm [PDF]

open access: yes, 2015
Diabetic Retinopathy is an eye disease where in which veins may swell and release liquid or new irregular veins develop on retina and piece the light touchy part, this will prompt vision misfortune.
, Dileep J, Manohar P
core   +2 more sources

Metabolic Dysfunction in New‐Onset Idiopathic Intracranial Hypertension: Identification of Novel Biomarkers

open access: yesAnnals of Neurology, Volume 96, Issue 3, Page 595-607, September 2024.
Objective Idiopathic intracranial hypertension (IIH) is a neurometabolic disease with an increasing incidence. The pathophysiology is unknown, but improvement of diagnosis and management requires discovery of novel biomarkers. Our objective was to identify such candidate biomarkers in IIH, and secondarily, test for associations between identified ...
Johanne Juhl Korsbæk   +10 more
wiley   +1 more source

Visual and Ocular Manifestations of Alzheimer's Disease and Their Use as Biomarkers for Diagnosis and Progression [PDF]

open access: yes, 2016
Alzheimer's disease (AD) is the most common form of dementia affecting the growing aging population today, with prevalence expected to rise over the next 35 years.
Brenton, J   +3 more
core   +1 more source

Evaluation of Peripapillary and Macular Vascular Flow Changes with OCT-A in Patients with Superficial Optic Disk Drusen. [PDF]

open access: yesSisli Etfal Hastan Tip Bul, 2022
Turker IC   +6 more
europepmc   +1 more source

Optic Disc Drusen in Patients With Ocular Hypertension: A Case Series and Review of the Literature. [PDF]

open access: yesJ Neuroophthalmol, 2022
Kohli D   +4 more
europepmc   +1 more source

Autosomal Dominant Retinal Dystrophies Caused by a Founder Splice Site Mutation, c.828+3A>T, in PRPH2 and Protein Haplotypes in trans as Modifiers. [PDF]

open access: yes, 2016
PurposeWe determined the phenotypic variation, disease progression, and potential modifiers of autosomal dominant retinal dystrophies caused by a splice site founder mutation, c.828+3A>T, in the PRPH2 gene.MethodsA total of 62 individuals (19 families)
Birch, David G   +7 more
core  

VISI KOMPUTER UNTUK DETEKSI EKSUDAT PADA PENDERITA DIABETIC RETINOPATHY [PDF]

open access: yes, 2012
Diabetes mellitus merupakan penyakit yang menyerang darah manusia dimana kadar gula dalam darah melebihi normal. Komplikasi mata akibat diabetes atau yang sering dikenal dengan istilah diabetic retinopathy antara lain eksudat lunak, eksudat keras ...
Fetty , Tri Anggraeny
core  

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